Yifat Alcalay
Overview
Explore the profile of Yifat Alcalay including associated specialties, affiliations and a list of published articles.
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Articles
26
Citations
285
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0
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Recent Articles
1.
Maayan Eshed G, Levinson T, Mina Y, Ashkenazi A, Dekel M, Cohen-Poradosu R, et al.
J Neurol Sci
. 2024 Nov;
467:123286.
PMID: 39550785
Purpose: To compare functional outcomes and help differentiate between important causative agents of acute infectious encephalitis in adults, focusing on West Nile virus encephalitis (WNVE). Methods: The electronic database of...
2.
Omer N, Droby A, Silbak R, Trablus N, Bar David A, Shiner T, et al.
J Neurol Neurosurg Psychiatry
. 2024 Jul;
PMID: 39084863
Background: MRI is an important tool for disease diagnosis of Creutzfeldt-Jakob disease (CJD), yet its role in identifying preclinical stages of disease remains unclear. Here, we explored subtle white matter...
3.
Segal Y, Rotschild O, Mina Y, Maayan Eshed G, Levinson T, Paran Y, et al.
Ann Clin Transl Neurol
. 2024 Jul;
11(9):2337-2349.
PMID: 39030965
Objectives: The incidence of autoimmune encephalitis (AIE) has risen in the last decade, yet recent studies are lacking. We compared the epidemiology of autoimmune and infectious encephalitis cases in Tel-Aviv...
4.
Gadoth A, Nisnboym M, Alcalay Y, Zubkov A, Schwartz I, Schwartz D, et al.
Neurol Neuroimmunol Neuroinflamm
. 2023 Aug;
10(6).
PMID: 37591767
Background And Objectives: Antileucine-rich glioma-inactivated 1 (anti-LGI1) autoimmune encephalitis was first described in 2010 and is today the most common type of limbic encephalitis. During the course of the disease,...
5.
Bregman N, Shiner T, Kave G, Alcalay R, Gana-Weisz M, Goldstein O, et al.
BMC Neurol
. 2023 Jun;
23(1):229.
PMID: 37312066
No abstract available.
6.
Bregman N, Shiner T, Kave G, Alcalay R, Gana-Weisz M, Goldstein O, et al.
BMC Neurol
. 2023 Apr;
23(1):151.
PMID: 37069531
Background: Creutzfeldt-Jakob Disease (CJD) is the most common prion disease in humans causing a rapidly progressive neurological decline and dementia and is invariably fatal. The familial forms (genetic CJD, gCJD)...
7.
Segal Y, Nisnboym M, Regev K, Arnon K, Kolb H, Fahoum F, et al.
Neurol Neuroimmunol Neuroinflamm
. 2023 Mar;
10(3).
PMID: 36973076
Background And Objectives: To explore the clinical characteristics and HLA associations of patients with anti-leucine-rich glioma-inactivated 1 encephalitis (LGI1E) from a large single center in Israel. Anti-LGI1E is the most...
8.
Saiag E, Alcalay Y, Marudi O, Orr-Urtreger A, Hagin D
Vaccine
. 2022 Dec;
41(4):914-921.
PMID: 36572602
With the emergence of the severe acute respiratory syndrome 2 (SARS-CoV-2) B.1.1.529/BA.1 (Omicron) variant in early 2022, Israel began vaccinating individuals 6o years of age or older with a fourth...
9.
Krivitski D, Alcalay Y, Peer M, Paran Y, Eisenstein O, Davidson T, et al.
Neurol Sci
. 2022 Sep;
44(1):369-372.
PMID: 36112277
Background: Paraneoplastic neurological syndromes have diverse clinical presentations and offer an opportunity for early diagnosis of malignancy and treatment. Recently, a new paraneoplastic syndrome associated with seminoma was described, consisting...
10.
Freund T, Baxter S, Walsh T, Golan H, Kapelushnik J, Abramsohn-Goldenberg M, et al.
J Clin Immunol
. 2022 Sep;
43(1):151-164.
PMID: 36063261
Pathogenic variants in LRBA, encoding the LPS Responsive Beige-Like Anchor (LRBA) protein, are responsible for recessive, early-onset hypogammaglobulinemia, severe multi-organ autoimmunity, and lymphoproliferation, with increased risk for malignancy. LRBA deficiency...